Efficacy of re-treatment with TMC435 as combination therapy in hepatitis C virus-infected patients following TMC435 monotherapy.
Identifieur interne : 000A12 ( Ncbi/Checkpoint ); précédent : 000A11; suivant : 000A13Efficacy of re-treatment with TMC435 as combination therapy in hepatitis C virus-infected patients following TMC435 monotherapy.
Auteurs : Oliver Lenz [Belgique] ; Joep De Bruijne ; Leen Vijgen ; Thierry Verbinnen ; Christine Weegink ; Herwig Van Marck ; Ina Vandenbroucke ; Monika Peeters ; Kenneth Simmen ; Greg Fanning ; Rene Verloes ; Gaston Picchio ; Hendrik ReesinkSource :
- Gastroenterology ; 2012.
English descriptors
- KwdEn :
- Antiviral Agents (therapeutic use), Drug Resistance, Viral, Drug Therapy, Combination, Genotype, Hepacivirus (genetics), Hepatitis C (blood), Hepatitis C (drug therapy), Hepatitis C (virology), Heterocyclic Compounds, 3-Ring (therapeutic use), Humans, Interferon-alpha (therapeutic use), Male, Mutation, Polyethylene Glycols (therapeutic use), Protease Inhibitors (therapeutic use), RNA, Viral (blood), RNA, Viral (drug effects), Recombinant Proteins (therapeutic use), Ribavirin (therapeutic use), Simeprevir, Sulfonamides (therapeutic use), Viral Load.
- MESH :
- chemical , blood : RNA, Viral.
- chemical , drug effects : RNA, Viral.
- chemical , therapeutic use : Antiviral Agents, Heterocyclic Compounds, 3-Ring, Interferon-alpha, Polyethylene Glycols, Protease Inhibitors, Recombinant Proteins, Ribavirin, Sulfonamides.
- blood : Hepatitis C.
- drug therapy : Hepatitis C.
- genetics : Hepacivirus.
- virology : Hepatitis C.
- Drug Resistance, Viral, Drug Therapy, Combination, Genotype, Humans, Male, Mutation, Simeprevir, Viral Load.
Abstract
In the TMC435-C101 study, 6 patients infected with hepatitis C virus genotype 1 were treated with the protease inhibitor TMC435 (200 mg once daily) as monotherapy for 5 days. Approximately 1.5 years later, 5 of these patients were re-treated with TMC435 (200 mg once daily) plus pegylated interferon alfa-2a and ribavirin (PegIFNα-2a and RBV) for 4 weeks, followed by PegIFNα-2a and RBV until week 48 (in the Optimal Protease inhibitor Enhancement of Response to therApy [OPERA-1] study). TMC435-resistant variants, which emerged in all 5 patients during the TMC435-C101 study, were no longer detected at the beginning of the OPERA-1 study based on virus population sequencing. During the OPERA-1 study, 3 patients had a sustained virologic response; deep sequencing indicated low-level persistence of resistant variants in the remaining 2 patients, which might have affected their response to re-treatment.
DOI: 10.1053/j.gastro.2012.07.117
PubMed: 22885330
Affiliations:
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pubmed:22885330Le document en format XML
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<series><title level="j">Gastroenterology</title>
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<term>Hepacivirus (genetics)</term>
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<term>Hepatitis C (drug therapy)</term>
<term>Hepatitis C (virology)</term>
<term>Heterocyclic Compounds, 3-Ring (therapeutic use)</term>
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<term>Interferon-alpha (therapeutic use)</term>
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<term>Mutation</term>
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<term>RNA, Viral (blood)</term>
<term>RNA, Viral (drug effects)</term>
<term>Recombinant Proteins (therapeutic use)</term>
<term>Ribavirin (therapeutic use)</term>
<term>Simeprevir</term>
<term>Sulfonamides (therapeutic use)</term>
<term>Viral Load</term>
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<front><div type="abstract" xml:lang="en">In the TMC435-C101 study, 6 patients infected with hepatitis C virus genotype 1 were treated with the protease inhibitor TMC435 (200 mg once daily) as monotherapy for 5 days. Approximately 1.5 years later, 5 of these patients were re-treated with TMC435 (200 mg once daily) plus pegylated interferon alfa-2a and ribavirin (PegIFNα-2a and RBV) for 4 weeks, followed by PegIFNα-2a and RBV until week 48 (in the Optimal Protease inhibitor Enhancement of Response to therApy [OPERA-1] study). TMC435-resistant variants, which emerged in all 5 patients during the TMC435-C101 study, were no longer detected at the beginning of the OPERA-1 study based on virus population sequencing. During the OPERA-1 study, 3 patients had a sustained virologic response; deep sequencing indicated low-level persistence of resistant variants in the remaining 2 patients, which might have affected their response to re-treatment.</div>
</front>
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<tree><noCountry><name sortKey="De Bruijne, Joep" sort="De Bruijne, Joep" uniqKey="De Bruijne J" first="Joep" last="De Bruijne">Joep De Bruijne</name>
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<name sortKey="Peeters, Monika" sort="Peeters, Monika" uniqKey="Peeters M" first="Monika" last="Peeters">Monika Peeters</name>
<name sortKey="Picchio, Gaston" sort="Picchio, Gaston" uniqKey="Picchio G" first="Gaston" last="Picchio">Gaston Picchio</name>
<name sortKey="Reesink, Hendrik" sort="Reesink, Hendrik" uniqKey="Reesink H" first="Hendrik" last="Reesink">Hendrik Reesink</name>
<name sortKey="Simmen, Kenneth" sort="Simmen, Kenneth" uniqKey="Simmen K" first="Kenneth" last="Simmen">Kenneth Simmen</name>
<name sortKey="Van Marck, Herwig" sort="Van Marck, Herwig" uniqKey="Van Marck H" first="Herwig" last="Van Marck">Herwig Van Marck</name>
<name sortKey="Vandenbroucke, Ina" sort="Vandenbroucke, Ina" uniqKey="Vandenbroucke I" first="Ina" last="Vandenbroucke">Ina Vandenbroucke</name>
<name sortKey="Verbinnen, Thierry" sort="Verbinnen, Thierry" uniqKey="Verbinnen T" first="Thierry" last="Verbinnen">Thierry Verbinnen</name>
<name sortKey="Verloes, Rene" sort="Verloes, Rene" uniqKey="Verloes R" first="Rene" last="Verloes">Rene Verloes</name>
<name sortKey="Vijgen, Leen" sort="Vijgen, Leen" uniqKey="Vijgen L" first="Leen" last="Vijgen">Leen Vijgen</name>
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